Erythrocyte anti-oxyenzyme activity in preterm infants with retinopathy of prematurity.

Neonatology

Graduate Institute of Clinical Medical Sciences, Chang Gung Children's Hospital, Chang Gung University, Taoyuan, Taiwan.

Published: August 2007

AI Article Synopsis

  • - The study investigates Retinopathy of Prematurity (ROP), a major cause of visual impairment in premature infants, focusing on the relationship between antioxidant enzyme activity in their red blood cells and ROP incidence.
  • - Researchers collected blood samples from 33 preterm infants and found that lower levels of glutathione peroxidase activity, along with factors like gestational age and birth weight, were linked to the presence of ROP.
  • - The findings suggest that while certain clinical factors are risk indicators for ROP, no direct correlation was observed between enzyme activity and the severity of ROP in this study.

Article Abstract

Background: Retinopathy of prematurity (ROP) is the main cause of visual impairment in premature infants and is considered to be a multifactorial disease. Because of the similarity between the human retina and the erythrocyte concerning their antioxidant mechanism, the aim of this study was to measure the erythrocyte anti-oxyenzyme activity of preterm infants.

Methods: This prospective study was performed on a tertiary referral hospital. Blood samples were collected from umbilical arterial lines or the radial artery of 33 preterm infants within 24 h after delivery to evaluate erythrocyte anti-oxyenzyme activity. Clinical data and oxygen administration were obtained and the correlations of enzyme activity and ROP status were examined.

Results: Gestational age, birth weight, 1-min Apgar score, and cellular glutathione peroxidase activity were significantly lower in preterm infants with ROP. There was no correlation between enzyme activity and gestational age, birth weight, or severity of ROP. There were no differences in cumulative oxygen and ventilator administration.

Conclusions: Gestational age and birth weight, 1-min Apgar score, and glutathione peroxidase activity are risk factors for ROP. Defective glutathione peroxidase activity may contribute to the initial phase of ROP.

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Source
http://dx.doi.org/10.1159/000100087DOI Listing

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